HIV/AIDS Clinical Trial
— I-TESTOfficial title:
The 4 Youth by Youth Project: A Pragmatic Stepped-wedge Cluster Randomized Controlled Trial to Expand Youth-friendly HIV Self-testing Services in Nigeria
Verified date | December 2023 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The current study extends the study team's earlier efforts described in ClinicalTrail ID#: NCT04070287 and NCT03874663. The I-TEST (Innovative Tools to Expand Youth-friendly HIV Self-Testing) study known locally as the 4 Youth by Youth project, sought to develop and evaluate novel youth-friendly HIVST services in Nigeria using open challenges and apprenticeship training informed by a participatory learning collaborative model. The study thus aims to reach young Nigerians that remain undiagnosed for HIV and to facilitate linkage and retention in preventive services (includes STI testing/treatment, PrEP referral, condom use).
Status | Active, not recruiting |
Enrollment | 1500 |
Est. completion date | April 1, 2024 |
Est. primary completion date | April 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 14 Years to 24 Years |
Eligibility | Inclusion Criteria: - Age 14-24 - Self-reported HIV negative or unknown HIV status - Currently and planning on residing in one of the 30 areas during the next 12 months - Able to complete the survey in English (the national language of Nigeria) - All participants must agree to informed consent and provide their cell mobile number for follow-up and retention Exclusion Criteria: - Younger than 14 and older than 24 - Inability to comply with the study protocol - Illness, cognitive impairment, or threatening behavior with acute risk to self or others - No informed consent - No contact phone number |
Country | Name | City | State |
---|---|---|---|
Nigeria | Nigerian Institute of Medical Research | Yaba | Lagos |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Nigerian Institute of Medical Research, University of North Carolina, Chapel Hill |
Nigeria,
Iwelunmor J, Ezechi O, Obiezu-Umeh C, Gbaja-Biamila T, Nwaozuru U, Oladele D, Musa AZ, Idigbe I, Uzoaru F, Airhihenbuwa C, Muessig K, Conserve DF, Kapogiannis B, Tucker JD. The 4 youth by youth HIV self-testing crowdsourcing contest: A qualitative evaluation. PLoS One. 2020 May 29;15(5):e0233698. doi: 10.1371/journal.pone.0233698. eCollection 2020. — View Citation
Nwaozuru U, Iwelunmor J, Ong JJ, Salah S, Obiezu-Umeh C, Ezechi O, Tucker JD. Preferences for HIV testing services among young people in Nigeria. BMC Health Serv Res. 2019 Dec 27;19(1):1003. doi: 10.1186/s12913-019-4847-x. — View Citation
Obiezu-Umeh C, Gbajabiamila T, Ezechi O, Nwaozuru U, Ong JJ, Idigbe I, Oladele D, Musa AZ, Uzoaru F, Airhihenbuwa C, Tucker JD, Iwelunmor J. Young people's preferences for HIV self-testing services in Nigeria: a qualitative analysis. BMC Public Health. 2021 Jan 7;21(1):67. doi: 10.1186/s12889-020-10072-1. — View Citation
WHO/TDR. (2018). Crowdsourcing in Health and Health Research: A Practical Guide (TDR/STRA/18.4). Retrieved from Geneva: https://www.who.int/tdr/publications/year/2018/crowdsourcing-practical-guide/en/
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Key Implementation Factors | Guided by the RE-AIM framework for implementation science, semi-structured, in-depth interviews will be conducted at the individual and setting level to explore the factors associated with the implementation of the intervention (e.g., reach, adoption, implementation, and maintenance). | Up to 24 months | |
Primary | Uptake of HIV Self-testing | The number of persons who tested with an HIV self-test among the total number of participants in the study. The primary outcome will be ascertained using a photographic verification approach via a mobile application or a USSD (Unstructured Supplementary Service Data) system to verify the HIVST results. The number of persons who tested with an HIV self-test | Up to 24 months | |
Secondary | Uptake of Facility-Based HIV testing | The number of persons who received an HIV test at a youth-friendly clinic among the total number of participants in the study. | Up to 24 months | |
Secondary | Sexually Transmitted Infection (STI) Testing | The number of persons who completed a consultation at the youth-friendly clinic for STI testing. In addition, the baseline and follow-up surveys include items on knowledge and testing of sexually transmitted infections (gonorrhea, chlamydia, syphilis, and hepatitis B virus). | Up to 24 months | |
Secondary | Sexually Transmitted Infection (STI) Treatment | The number of persons initiating STI treatment among the total number of persons with active infection linked to care. | Up to 24 months | |
Secondary | PrEP Referral | PrEP referral will be assessed based on the proportion of participants who are "optimal" (assessed based on the sexual behavioral history and willingness to use PrEP) candidates for PrEP referral and the total number of participants referred for PrEP initiation at the health care facilities. | Up to 24 months | |
Secondary | 100% Condom Use | The baseline and follow-up survey includes items on condom usage in the last sexual intercourse and a 4-item Condom Use Self Efficacy Scale. | Up to 24 months | |
Secondary | Youth Engagement | A 12-item scale on youth engagement will be used to assess the HIV prevention services proposed by the youth teams. The scale was adapted from the 20-item Tiffany-Eckenrode Program Participation Scale (TEPPS). Responses to the participation items were measured on a 5-point Likert-type scale, ranging from "strongly disagree (0)" to "Strongly agree (4)". Higher TEPPS scores indicate higher levels of program participation. The item is only included in the follow-up survey. | Up to 24 months | |
Secondary | Cost effectiveness of the intervention | The incremental cost-effectiveness ratio of participants involved in the I-TEST intervention phase compared to the control phase. | Up to 24 months |
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